Evidence map›Paper›PMID 30126206›Full record

ArticleMolecules (Basel, Switzerland)2018

Green Tea Catechin Is an Alternative Immune Checkpoint Inhibitor that Inhibits PD-L1 Expression and Lung Tumor Growth.

Anchalee Rawangkan, Pattama Wongsirisin, Kozue Namiki, Keisuke Iida, Yasuhito Kobayashi, Yoshihiko Shimizu, Hirota Fujiki, Masami Suganuma

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed, 2 pooled it
9.0field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

72 citing papers in PubMed, 2 syntheses or guidelines pooled it, 141 citations in OpenAlex.

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  8. Optogenetic engineering for precision cancer immunotherapy.Trends in pharmacological sciences · 2025
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12 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 1 country.

Anchalee RawangkanGraduate School of Science and Engineering, Saitama University, Saitama 338-8570, Japan. ewmedsci@gmail.com.ORCID 0000-0003-1620-756X
Pattama WongsirisinGraduate School of Science and Engineering, Saitama University, Saitama 338-8570, Japan. wongsiri.patt@gmail.com.ORCID 0000-0001-7884-2484
Kozue NamikiGraduate School of Science and Engineering, Saitama University, Saitama 338-8570, Japan. k.namiki1080@gmail.com.
Keisuke IidaMolecular Chirality Research Center and Department of Chemistry, Graduate School of Science, Chiba University, Chiba 263-8522, Japan. kiida@chiba-u.jp.
Yasuhito KobayashiSaitama Cardiovascular and Respiratory Center, Kumagaya, Saitama 360-0197, Japan. kobayashiyasuhito@yahoo.co.jp.
Yoshihiko ShimizuSaitama Cardiovascular and Respiratory Center, Kumagaya, Saitama 360-0197, Japan. shimizu.yoshihiko@pref.saitama.lg.jp.
Hirota FujikiFaculty of Medicine, Saga University, Saga 849-8501, Japan. uv4h-fjk@asahi-net.or.jp.
Masami SuganumaGraduate School of Science and Engineering, Saitama University, Saitama 338-8570, Japan. masami0306@mail.saitama-u.ac.jp.ORCID 0000-0002-4257-6695
Saitama Cancer Center · JPSaitama Prefecture · JPChiba University · JPSaga University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The anticancer activity of immune checkpoint inhibitors is attracting attention in various clinical sites. Since green tea catechin has cancer-preventive activity in humans, whether green tea catechin supports the role of immune checkpoint inhibitors was studied. We here report that (-)-epigallocatechin gallate (EGCG) inhibited programmed cell death ligand 1 (PD-L1) expression in non⁻small-cell lung cancer cells, induced by both interferon (IFN)-γ and epidermal growth factor (EGF). The mRNA and protein levels of IFN-γ⁻induced PD-L1 were reduced 40⁻80% after pretreatment with EGCG and green tea extract (GTE) in A549 cells, via inhibition of JAK2/STAT1 signaling. Similarly, EGF-induced PD-L1 expression was reduced about 37⁻50% in EGCG-pretreated Lu99 cells through inhibition of EGF receptor/Akt signaling. Furthermore, 0.3% GTE in drinking water reduced the average number of tumors per mouse from 4.1 ± 0.5 to 2.6 ± 0.4 and the percentage of PD-L1 positive cells from 9.6% to 2.9%, a decrease of 70%, in lung tumors of A/J mice given a single intraperitoneal injection of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK). In co-culture experiments using F10-OVA melanoma cells and tumor-specific CD3+ T cells, EGCG reduced

Indexed as

AnimalsAntineoplastic Agents, PhytogenicB7-H1 AntigenCatechinCell Line, TumorDisease Models, AnimalGene ExpressionHumansImmunomodulationLung NeoplasmsMicePhosphorylationProto-Oncogene Proteins c-aktSignal TransductionSTAT1 Transcription FactorTeaAntineoplastic Agents, PhytogenicB7-H1 AntigenCatechinCD274 protein, humanProto-Oncogene Proteins c-aktSTAT1 protein, humanSTAT1 Transcription FactorTeaepidermal growth factor(−)-epigallocatechin gallateimmune checkpointinterferon-γlung tumor

Identifiers

PMID30126206
PMCPMC6222340
OpenAlexW2887862366

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.